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Beer’s Law
By- Krishan Kumar Verma, Assistant Professor
Ram-Eesh Institute of Vocational & Technical Education
Learning Outcomes:
The learners will be able to-
β€’ Define Beer’s law
β€’ Derive Beer’s law
Introduction
β€’ UV-Visible spectroscopy is a type of absorption spectroscopy.
β€’ Absorption spectroscopy involves measurement of absorbance or
transmittance of sample contained in a transparent cell with path length
of b cm.
β€’ Absorbance is inversely proportional to transmittance.
β€’ Absorption of light is mainly governed by Beer’s law
A = log
1
T
= βˆ’ log T = log (Po/P) = Ξ΅ b c
A = Absorbance
T = Transmittance
P0 = Incident radiant power
P = Transmitted radiant power
Ξ΅ = Molar absorptivity (previously molar extinction coefficient)
b = Path length of sample cell(cm)
C = Concentration of sample (mol L-1)
Derivation of Beer’s law:
P0 = Incident radiant power
P = Transmitted radiant power
n = number of absorbing atoms, ions or molecules
b = path length of sample cell
S = cross section area of block
dx = thickness of block
dn = number of absorbing particles in the block
dS = Total area of photon absorption surface
b
P0 P
n
dx
Sdn
β€’ The ratio of photon capture are to the total area =
dS
S
This represents the probability for capture of photon with in the section.
β€’ The power of beam entering the section, Px, is proportional to the
number of photons per unit area and dPx represents the power
absorbed with in the section.
Therefore, the fraction absorbed = βˆ’
dPx
Px
(- sign indicates decrease in power after absorption)
β€’ This ratio is equal to the average probability of photon capture;
βˆ’
𝑑𝑃π‘₯
𝑃π‘₯
=
𝑑𝑆
𝑆
1
dS Ξ± dn
dS = a dn
Replacing the dS to equation 1,
βˆ’
𝑑𝑃π‘₯
𝑃π‘₯
=
π‘Ž 𝑑𝑛
𝑆
βˆ’ ln
𝑃
𝑃0
=
π‘Ž 𝑛
𝑆
log
𝑃0
𝑃
=
π‘Ž 𝑛
2.303 𝑆
𝑃0
𝑃
𝑑𝑃π‘₯
𝑃π‘₯
=
0
𝑛
π‘Ž 𝑑𝑛
𝑆
log
𝑃0
𝑃
=
π‘Ž 𝑛
2.303 𝑆
log
𝑃0
𝑃
=
π‘Ž 𝑛 𝑏
2.303 𝑉
𝑠𝑖𝑛𝑐𝑒, 𝑆 =
𝑉 π‘π‘š3
𝑏 π‘π‘š
Now
𝑛
𝑉
may be converted to concentration (mol L-1)
Number of mol =
n particles
6.022 x 1023 particles per mol
C = π‘π‘’π‘šπ‘π‘’π‘Ÿ π‘œπ‘“ π‘šπ‘œπ‘™π‘’π‘ 
πΏπ‘–π‘‘π‘Ÿπ‘’π‘ 
=
n particles
6.022 x 1023 particles per mol
1000 cm3 Lβˆ’1
V cm3
2
After replacing
𝑛
𝑉
concentration (mol/L)
log
𝑃0
𝑃
=
6.022 x 1023
π‘Ž 𝑏 𝑐
2.303 x 1000
Finally, after combining all the constants;
log
𝑃0
𝑃
= Ξ΅ b c = A (Beer’s law equation)
Ξ΅ = molar absorptivity
For multicomponent systems:
β€’ When more than one absorbing species are present.
β€’ The absorbing species must not interact with each other.
Total absorbance (A Total) = A1 + A2 + A3 + …………….An
= Ξ΅1bc + Ξ΅2bc + Ξ΅3bc + ……………. Ξ΅nbc
Limitations & Deviations-
Beer’s Law
By- Krishan Kumar Verma, Assistant Professor
Ram-Eesh Institute of Vocational & Technical Education
Limitations to Beer’s law:
According to Beer’s law, A Ξ± C (linear relation)
Concentration
Absorbance
Real limitations to Beer’s law:
β€’ Beer’s law is applicable only at very low concentration (≀ 0.01M).
β€’ At high concentrations, average distance between molecules or ions
decreases.
β€’ The solute-solute, solute-solvent, hydrogen bonding and electrostatic
interactions may increase that can alter absorptivity and hence may
cause deviations from linear relation.
β€’ Absorptivity also depends on refractive index of the medium, that can
be altered by varying concentration.
Correction to be done: use
Ξ΅ 𝑛
𝑛2
+2 2 instead of Ξ΅
Apparent chemical deviations:
β€’ Involves dissociation or association of analyte.
β€’ Reaction of analyte with solvent to produce a product with different
absorption spectrum than analyte.
e.g. In acid-base indicators
HIn H+ + In-
(color I) (color II)
For unbuffered solution,
At 430 nm, absorption is due to In-
At 570 nm, absorption is due to HIn
Indicator concentration
Absorbance
-ve deviation
(at 570 nm)
+ve deviation
(at 430 nm)
Instrumental deviations:
1. Due to polychromatic radiation:
Consider a beam with two wavelength, λ’ and λ’’
For λ’
A’ = Ρ’ b c
𝑃0
β€²
𝑃′ = 10 -Ρ’bc
P’ = P0’10 Ρ’bc
For λ’’
P’’ = P0’’10 Ρ’’bc
The overall combined absorbance can be written as-
Am = log (
𝑃0
β€²
+𝑃0
β€²β€²
𝑃′
+𝑃′′ )
Am = log
(𝑃0
β€²+𝑃0
β€²β€²)
(𝑃0
β€²10
_
Ξ΅bc + 𝑃 0
β€²β€²
10
_
Ξ΅β€²β€²bc)
When molar absorptivity's are same at two wavelengths, Beer’s law is
followed.
Am = Ξ΅β€²bc = Ξ΅β€²β€²bc
But when Ξ΅β€² and Ρ′’ are not equal, relationship becomes non linear.
Concentration
Absorbance
Ξ΅β€² = Ξ΅β€²β€² = 1000
Ξ΅β€² = 1500, Ξ΅β€²β€² = 500
Ξ΅β€² = 1750, Ξ΅β€²β€² = 250
2. Due to stray radiation:
β€’ Radiation coming from monochromator is usualy contaminated with
small amounts of scattered or stray radiation.
β€’ Stray light is the radiation from instrument that is outside the nominal
wavelength band chosen for determination.
β€’ Stray light may be observed due to scattering, reflections of gratings
surfaces, lens or mirrors.
β€’ Stray radiation wavelength often differs from principal radiation and
may not have passed through sample.
β€’ Necessary correction:
A’ = log (
𝑃0+𝑃𝑆
𝑃+𝑃𝑆
)
PS = power of stray radiation
3. Due to mismatched cell:
β€’ Mismatch between analyte and blank cell.
β€’ Unequal path lengths and optical properties
β€’ Can be corrected by linear regression, use of single beam instrument
or addition of intercept in Beer’s law equation.
A = Ξ΅bc + k
Concentration
Absorbance
0 %
0.2 %
1 %
5 %
𝑃 𝑆
𝑃0
x100 %
THANK YOU

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Beer's law -Derivation & Deviations

  • 1. Beer’s Law By- Krishan Kumar Verma, Assistant Professor Ram-Eesh Institute of Vocational & Technical Education
  • 2. Learning Outcomes: The learners will be able to- β€’ Define Beer’s law β€’ Derive Beer’s law
  • 3. Introduction β€’ UV-Visible spectroscopy is a type of absorption spectroscopy. β€’ Absorption spectroscopy involves measurement of absorbance or transmittance of sample contained in a transparent cell with path length of b cm. β€’ Absorbance is inversely proportional to transmittance. β€’ Absorption of light is mainly governed by Beer’s law
  • 4. A = log 1 T = βˆ’ log T = log (Po/P) = Ξ΅ b c A = Absorbance T = Transmittance P0 = Incident radiant power P = Transmitted radiant power Ξ΅ = Molar absorptivity (previously molar extinction coefficient) b = Path length of sample cell(cm) C = Concentration of sample (mol L-1)
  • 5. Derivation of Beer’s law: P0 = Incident radiant power P = Transmitted radiant power n = number of absorbing atoms, ions or molecules b = path length of sample cell S = cross section area of block dx = thickness of block dn = number of absorbing particles in the block dS = Total area of photon absorption surface b P0 P n dx Sdn
  • 6. β€’ The ratio of photon capture are to the total area = dS S This represents the probability for capture of photon with in the section. β€’ The power of beam entering the section, Px, is proportional to the number of photons per unit area and dPx represents the power absorbed with in the section. Therefore, the fraction absorbed = βˆ’ dPx Px (- sign indicates decrease in power after absorption) β€’ This ratio is equal to the average probability of photon capture; βˆ’ 𝑑𝑃π‘₯ 𝑃π‘₯ = 𝑑𝑆 𝑆 1
  • 7. dS Ξ± dn dS = a dn Replacing the dS to equation 1, βˆ’ 𝑑𝑃π‘₯ 𝑃π‘₯ = π‘Ž 𝑑𝑛 𝑆 βˆ’ ln 𝑃 𝑃0 = π‘Ž 𝑛 𝑆 log 𝑃0 𝑃 = π‘Ž 𝑛 2.303 𝑆 𝑃0 𝑃 𝑑𝑃π‘₯ 𝑃π‘₯ = 0 𝑛 π‘Ž 𝑑𝑛 𝑆
  • 8. log 𝑃0 𝑃 = π‘Ž 𝑛 2.303 𝑆 log 𝑃0 𝑃 = π‘Ž 𝑛 𝑏 2.303 𝑉 𝑠𝑖𝑛𝑐𝑒, 𝑆 = 𝑉 π‘π‘š3 𝑏 π‘π‘š Now 𝑛 𝑉 may be converted to concentration (mol L-1) Number of mol = n particles 6.022 x 1023 particles per mol C = π‘π‘’π‘šπ‘π‘’π‘Ÿ π‘œπ‘“ π‘šπ‘œπ‘™π‘’π‘  πΏπ‘–π‘‘π‘Ÿπ‘’π‘  = n particles 6.022 x 1023 particles per mol 1000 cm3 Lβˆ’1 V cm3 2
  • 9. After replacing 𝑛 𝑉 concentration (mol/L) log 𝑃0 𝑃 = 6.022 x 1023 π‘Ž 𝑏 𝑐 2.303 x 1000 Finally, after combining all the constants; log 𝑃0 𝑃 = Ξ΅ b c = A (Beer’s law equation) Ξ΅ = molar absorptivity
  • 10. For multicomponent systems: β€’ When more than one absorbing species are present. β€’ The absorbing species must not interact with each other. Total absorbance (A Total) = A1 + A2 + A3 + …………….An = Ξ΅1bc + Ξ΅2bc + Ξ΅3bc + ……………. Ξ΅nbc
  • 11. Limitations & Deviations- Beer’s Law By- Krishan Kumar Verma, Assistant Professor Ram-Eesh Institute of Vocational & Technical Education
  • 12. Limitations to Beer’s law: According to Beer’s law, A Ξ± C (linear relation) Concentration Absorbance
  • 13. Real limitations to Beer’s law: β€’ Beer’s law is applicable only at very low concentration (≀ 0.01M). β€’ At high concentrations, average distance between molecules or ions decreases. β€’ The solute-solute, solute-solvent, hydrogen bonding and electrostatic interactions may increase that can alter absorptivity and hence may cause deviations from linear relation. β€’ Absorptivity also depends on refractive index of the medium, that can be altered by varying concentration. Correction to be done: use Ξ΅ 𝑛 𝑛2 +2 2 instead of Ξ΅
  • 14. Apparent chemical deviations: β€’ Involves dissociation or association of analyte. β€’ Reaction of analyte with solvent to produce a product with different absorption spectrum than analyte. e.g. In acid-base indicators HIn H+ + In- (color I) (color II) For unbuffered solution, At 430 nm, absorption is due to In- At 570 nm, absorption is due to HIn Indicator concentration Absorbance -ve deviation (at 570 nm) +ve deviation (at 430 nm)
  • 15. Instrumental deviations: 1. Due to polychromatic radiation: Consider a beam with two wavelength, λ’ and λ’’ For λ’ A’ = Ρ’ b c 𝑃0 β€² 𝑃′ = 10 -Ρ’bc P’ = P0’10 Ρ’bc For λ’’ P’’ = P0’’10 Ρ’’bc The overall combined absorbance can be written as- Am = log ( 𝑃0 β€² +𝑃0 β€²β€² 𝑃′ +𝑃′′ )
  • 16. Am = log (𝑃0 β€²+𝑃0 β€²β€²) (𝑃0 β€²10 _ Ξ΅bc + 𝑃 0 β€²β€² 10 _ Ξ΅β€²β€²bc) When molar absorptivity's are same at two wavelengths, Beer’s law is followed. Am = Ξ΅β€²bc = Ξ΅β€²β€²bc But when Ξ΅β€² and Ρ′’ are not equal, relationship becomes non linear. Concentration Absorbance Ξ΅β€² = Ξ΅β€²β€² = 1000 Ξ΅β€² = 1500, Ξ΅β€²β€² = 500 Ξ΅β€² = 1750, Ξ΅β€²β€² = 250
  • 17. 2. Due to stray radiation: β€’ Radiation coming from monochromator is usualy contaminated with small amounts of scattered or stray radiation. β€’ Stray light is the radiation from instrument that is outside the nominal wavelength band chosen for determination. β€’ Stray light may be observed due to scattering, reflections of gratings surfaces, lens or mirrors. β€’ Stray radiation wavelength often differs from principal radiation and may not have passed through sample. β€’ Necessary correction: A’ = log ( 𝑃0+𝑃𝑆 𝑃+𝑃𝑆 ) PS = power of stray radiation
  • 18. 3. Due to mismatched cell: β€’ Mismatch between analyte and blank cell. β€’ Unequal path lengths and optical properties β€’ Can be corrected by linear regression, use of single beam instrument or addition of intercept in Beer’s law equation. A = Ξ΅bc + k Concentration Absorbance 0 % 0.2 % 1 % 5 % 𝑃 𝑆 𝑃0 x100 %